Cargando…

Chronically stimulated human MAIT cells are unexpectedly potent IL‐13 producers

Mucosal‐associated invariant T (MAIT) cells are unconventional T cells that recognize antigens derived from riboflavin biosynthesis. In addition to anti‐microbial functions, human MAIT cells are associated with cancers, autoimmunity, allergies and inflammatory disorders, although their role is poorl...

Descripción completa

Detalles Bibliográficos
Autores principales: Kelly, Jason, Minoda, Yosuke, Meredith, Tobias, Cameron, Garth, Philipp, Marie‐Sophie, Pellicci, Daniel G, Corbett, Alexandra J, Kurts, Christian, Gray, Daniel HD, Godfrey, Dale I, Kannourakis, George, Berzins, Stuart P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790710/
https://www.ncbi.nlm.nih.gov/pubmed/31323167
http://dx.doi.org/10.1111/imcb.12281
_version_ 1783458830270595072
author Kelly, Jason
Minoda, Yosuke
Meredith, Tobias
Cameron, Garth
Philipp, Marie‐Sophie
Pellicci, Daniel G
Corbett, Alexandra J
Kurts, Christian
Gray, Daniel HD
Godfrey, Dale I
Kannourakis, George
Berzins, Stuart P
author_facet Kelly, Jason
Minoda, Yosuke
Meredith, Tobias
Cameron, Garth
Philipp, Marie‐Sophie
Pellicci, Daniel G
Corbett, Alexandra J
Kurts, Christian
Gray, Daniel HD
Godfrey, Dale I
Kannourakis, George
Berzins, Stuart P
author_sort Kelly, Jason
collection PubMed
description Mucosal‐associated invariant T (MAIT) cells are unconventional T cells that recognize antigens derived from riboflavin biosynthesis. In addition to anti‐microbial functions, human MAIT cells are associated with cancers, autoimmunity, allergies and inflammatory disorders, although their role is poorly understood. Activated MAIT cells are well known for their rapid release of Th1 and Th17 cytokines, but we have discovered that chronic stimulation can also lead to potent interleukin (IL)‐13 expression. We used RNA‐seq and qRT‐PCR to demonstrate high expression of the IL‐13 gene in chronically stimulated MAIT cells, and directly identify IL‐13 using intracellular flow cytometry and multiplex bead analysis of MAIT cell cultures. This unexpected finding has important implications for IL‐13‐dependent diseases, such as colorectal cancer (CRC), that occur in mucosal areas where MAIT cells are abundant. We identify MAIT cells near CRC tumors and show that these areas and precancerous polyps express high levels of the IL‐13 receptor, which promotes tumor progression and metastasis. Our data suggest that MAIT cells have a more complicated role in CRC than currently realized and that they represent a promising new target for immunotherapies where IL‐13 can be a critical factor.
format Online
Article
Text
id pubmed-6790710
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-67907102019-10-21 Chronically stimulated human MAIT cells are unexpectedly potent IL‐13 producers Kelly, Jason Minoda, Yosuke Meredith, Tobias Cameron, Garth Philipp, Marie‐Sophie Pellicci, Daniel G Corbett, Alexandra J Kurts, Christian Gray, Daniel HD Godfrey, Dale I Kannourakis, George Berzins, Stuart P Immunol Cell Biol Outstanding Observation Mucosal‐associated invariant T (MAIT) cells are unconventional T cells that recognize antigens derived from riboflavin biosynthesis. In addition to anti‐microbial functions, human MAIT cells are associated with cancers, autoimmunity, allergies and inflammatory disorders, although their role is poorly understood. Activated MAIT cells are well known for their rapid release of Th1 and Th17 cytokines, but we have discovered that chronic stimulation can also lead to potent interleukin (IL)‐13 expression. We used RNA‐seq and qRT‐PCR to demonstrate high expression of the IL‐13 gene in chronically stimulated MAIT cells, and directly identify IL‐13 using intracellular flow cytometry and multiplex bead analysis of MAIT cell cultures. This unexpected finding has important implications for IL‐13‐dependent diseases, such as colorectal cancer (CRC), that occur in mucosal areas where MAIT cells are abundant. We identify MAIT cells near CRC tumors and show that these areas and precancerous polyps express high levels of the IL‐13 receptor, which promotes tumor progression and metastasis. Our data suggest that MAIT cells have a more complicated role in CRC than currently realized and that they represent a promising new target for immunotherapies where IL‐13 can be a critical factor. John Wiley and Sons Inc. 2019-07-19 2019-09 /pmc/articles/PMC6790710/ /pubmed/31323167 http://dx.doi.org/10.1111/imcb.12281 Text en © 2019 The Authors Immunology & Cell Biology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Outstanding Observation
Kelly, Jason
Minoda, Yosuke
Meredith, Tobias
Cameron, Garth
Philipp, Marie‐Sophie
Pellicci, Daniel G
Corbett, Alexandra J
Kurts, Christian
Gray, Daniel HD
Godfrey, Dale I
Kannourakis, George
Berzins, Stuart P
Chronically stimulated human MAIT cells are unexpectedly potent IL‐13 producers
title Chronically stimulated human MAIT cells are unexpectedly potent IL‐13 producers
title_full Chronically stimulated human MAIT cells are unexpectedly potent IL‐13 producers
title_fullStr Chronically stimulated human MAIT cells are unexpectedly potent IL‐13 producers
title_full_unstemmed Chronically stimulated human MAIT cells are unexpectedly potent IL‐13 producers
title_short Chronically stimulated human MAIT cells are unexpectedly potent IL‐13 producers
title_sort chronically stimulated human mait cells are unexpectedly potent il‐13 producers
topic Outstanding Observation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6790710/
https://www.ncbi.nlm.nih.gov/pubmed/31323167
http://dx.doi.org/10.1111/imcb.12281
work_keys_str_mv AT kellyjason chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers
AT minodayosuke chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers
AT meredithtobias chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers
AT camerongarth chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers
AT philippmariesophie chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers
AT pelliccidanielg chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers
AT corbettalexandraj chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers
AT kurtschristian chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers
AT graydanielhd chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers
AT godfreydalei chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers
AT kannourakisgeorge chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers
AT berzinsstuartp chronicallystimulatedhumanmaitcellsareunexpectedlypotentil13producers